Canonical Allele Identifier: CA349501152

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179415792C>G (hg19) ; chr2:g.178551065C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551065C>G , CM000664.2:g.178551065C>G	GRCh38
NC_000002.11:g.179415792C>G , CM000664.1:g.179415792C>G	GRCh37
NC_000002.10:g.179124038C>G	NCBI36
NG_011618.3:g.284738G>C , LRG_391:g.284738G>C
NG_051363.1:g.33239C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.83762G>C (TTN)	ENSP00000343764.6:p.Gly27921Ala
ENST00000342175.11:c.64847G>C (TTN)	ENSP00000340554.6:p.Gly21616Ala
ENST00000359218.10:c.64646G>C (TTN)	ENSP00000352154.5:p.Gly21549Ala
ENST00000342175.10:c.64847G>C (TTN)	ENSP00000340554.6:p.Gly21616Ala
ENST00000342992.10:c.83762G>C (TTN)	ENSP00000343764.6:p.Gly27921Ala
ENST00000359218.9:c.64646G>C (TTN)	ENSP00000352154.5:p.Gly21549Ala
ENST00000460472.6:c.64271G>C (TTN)	ENSP00000434586.1:p.Gly21424Ala
ENST00000589042.5:c.91466G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly30489Ala
ENST00000591111.5:c.86543G>C (TTN)	ENSP00000465570.1:p.Gly28848Ala
ENST00000615779.4:c.86543G>C (TTN)	ENSP00000483597.1:p.Gly28848Ala
NM_001256850.1:c.86543G>C (TTN)	NP_001243779.1:p.Gly28848Ala
NM_001267550.2:c.91466G>C (TTN) MANE Select	NP_001254479.2:p.Gly30489Ala
NM_003319.4:c.64271G>C (TTN)	NP_003310.4:p.Gly21424Ala
NM_133378.4:c.83762G>C (TTN)	NP_596869.4:p.Gly27921Ala
NM_133432.3:c.64646G>C (TTN)	NP_597676.3:p.Gly21549Ala
NM_133437.4:c.64847G>C (TTN)	NP_597681.4:p.Gly21616Ala
NR_038271.1:n.447-20235C>G (TTN-AS1)
NR_038272.1:n.2043+8704C>G (TTN-AS1)
XM_011511729.1:c.90563G>C (TTN)	XP_011510031.1:p.Gly30188Ala
XM_011511730.1:c.64457G>C (TTN)	XP_011510032.1:p.Gly21486Ala
XM_011511731.1:c.64316G>C (TTN)	XP_011510033.1:p.Gly21439Ala
XM_017004819.1:c.90359G>C (TTN)	XP_016860308.1:p.Gly30120Ala
XM_017004820.1:c.85757G>C (TTN)	XP_016860309.1:p.Gly28586Ala
XM_017004821.1:c.85754G>C (TTN)	XP_016860310.1:p.Gly28585Ala
XM_017004822.1:c.82796G>C (TTN)	XP_016860311.1:p.Gly27599Ala
XM_017004823.1:c.64412G>C (TTN)	XP_016860312.1:p.Gly21471Ala
XM_024453094.1:c.85907G>C (TTN)	XP_024308862.1:p.Gly28636Ala
XM_024453095.1:c.85904G>C (TTN)	XP_024308863.1:p.Gly28635Ala
XM_024453096.1:c.85337G>C (TTN)	XP_024308864.1:p.Gly28446Ala
XM_024453097.1:c.82679G>C (TTN)	XP_024308865.1:p.Gly27560Ala
XM_024453098.1:c.82598G>C (TTN)	XP_024308866.1:p.Gly27533Ala
XM_024453099.1:c.64361G>C (TTN)	XP_024308867.1:p.Gly21454Ala
XM_024453100.1:c.54215G>C (TTN)	XP_024308868.1:p.Gly18072Ala